MLS quiz cards Flashcards
Which of the following microcytic anemias has no relationship with iron metabolism?
- Iron deficiency anemia
*Sideroblastic anemia
*Anemia of chronic inflammation
*Thalassemia
Thalassemia is the correct answer.
*Thalassemia is a condition in which hemoglobin amino chains are reduced or deleted & has no direct relationship with iron metabolism.
*iron deficiency is a direct result of not having iron available for hemoglobin formation.
- Sideroblastic anemia results when iron is available but cannot be used for hemoglobin formation.
*Anemia of chronic inflammation occurs when iron is available in storage but cannot be released for use.
In what form must iron be when bound to hemoglobin for effective oxygen delivery?
- Ferrous ion
*Ferric ion
*Ferritin
*Transferrin
Ferrous ion is the correct answer
*Iron must be in the 2+ state (ferrous) to be able to bind & effectively deliver oxygen to the tissue.
*Iron in the 3+ state (ferric) is able to bind oxygen but does not release it effectively to the tissue.
*Ferritin is a form of storage iron & is not found in the erythrocyte.
- Transferrin is a transfer protein that delivers circulating iron to the tissues for storage or to developing erythrocytes for use.
The most common cause of iron deficiency worldwide is?
- Nutritional deficiency
*Chronic GI bleed
*Malabsorption
*Gastric bypass surgery
The correct answer is Malabsorption
*The most common cause of IDA worldwide is malabsorption, especially among women and children.
- Chronic GI bleeds, malabsorption syndromes, & gastric bypass surgery can all result in iron deficiency but are not as common as malabsorption.
You are analyzing a PCR run and see that one of your samples is a high positive but the internal control failed. What should you do?
*Result the sample as positive
*Result the sample as negative
*Result the sample as indeterminate
*Repeat the sample
This sample can be resulted as positive. The purpose of an internal control is to show amplification occurred. Internal controls add extra assurance to negative samples that they are true negatives. However, because this sample is positive, we know amplification occurred even without the internal control.
*The sample is positive, even though the internal control didn’t show up, therefore you would not result this sample as negative.
*Indeterminate results often occur from a sample being very low level positive, where you can not accurately differentiate between positive & negative. In this case the sample is a clear positive.
*This sample would not need to be repeated & can be resulted as is.
Which of the following EBV viral loads is least likely to be seen in a healthy individual?
*Undetected viral load
* 35 IU/mL
*75 IU/mL
*7,500 IU/mL
EBV is a virus that commonly affects children & then lays dormant in the body, being able to be detected at low circulating viral loads in most healthy adults. There is no definitive threshold for a clinically relevant EBV viral load, but higher viral loads are less likely to be seen in healthy individuals.
Uric acid is the final breakdown product of what two purines?
*Adenine & Thymine
*Thymine & Cytosine
*Adenine & Guanine
*Guanine & Thymine
The purines adenine & guanine are broken down into uric acid.
Cytosine & thymine are pyrimidines that are mostly broken down into ammonia, carbon dioxide, and water but not into uric acid
A culture was performed on a stool sample. After growth was obtained on the blood agar plate, the gram stain showed curved gram-negative rods. the oxidase, catalase, and urease were positive. What is the most likely bacterial identification?
*Helicobacter pylori
*Campylobacter concisus
*Helicobacter cinaedi
*Arcobacter spp.
the correct answer is Helicobacter pylori. Identification methods for curved gram-negative rods will include (in this order) oxidase, catalase, and urease. Helicobacter pylori will have the gram stain showing curved gram -negative rods. It will have positive results for oxidase, catalase, & urease.
Campylobacter concisus will have the gram stain showing curved gram-negative rods. It will have positive results for oxidase along with a negative catalase results.
Helicobacter cinaedi will have the gram stain showing curved gram-negative rods. It will have positive results for oxidase & catalase along with a negative urease test.
Arcobacter spp. will have the gram stain showing curved gram-negative rods. It will have positive results for oxidase & catalase along with a negative urease test.
How will unmethylated cytosine residues appear in a pyrogram after bisulfite treatment?
- As cytosine
- As uracil
- As thymine
- As guanine
Thymine is the correct answer.
bisulfite treatment converts unmethylated cytosine’s into uracil, which will then appear as thymine in the pyrogram, as the original DNA sequence would have thymine in it rather than uracil.
Any cytosine peaks in the pyrogram would be the results of methylated cytosine in the sequence.
A guanine peak would indicate a guanine nucleotide.
During DNA isolation, which of the following reagents is used to precipitate nucleic acids?
- TEMED
*Alcohols such as ethanol or isopropanol
*DEPC water
*Chloroform
Ethanol and Isopropanol are commonly used in molecular techniques for the precipitation of nucleic acids, DNA purification requires lysis of cells using NaOH & SDS; acidification using acetic acid and salt; extraction using phenol and chloroform; and lastly, precipitation of DNA which requires ethanol or isopropanol.
TEMED is tetramethylenediamine which is used as a catalyst for the solidification of polyacrylamide gels.
DEPC water is diethyl pyrocarbonate, a reagent that inactivates RNases.
Chloroform is used in the extraction step to solubilize DNA.
A stool specimen can be suspected of harboring Vibrio cholerae if it possesses which of the following characteristics?
- if the stool is well formed and shows blood steaks.
*if the stool is soft, dark, & positive for occult blood.
*if the stool contains a high concentration of segmented neutrophils.
*if the stool is watery with a high pH and flecks of mucus.
Diarrhea caused by V. cholera is watery & contains large concentrations of Na, bicarbonate, & other electrolytes, producing an alkaline pH. The diarrhea is caused by the action of cholera toxin on the intestinal epithelial cells, with the end results of stimulating adenyl cyclase ( cyclic AMP), which in turn inhibits the reabsorption of Na across the brush border membrane & stimulates the excretion of bicarbonate & potassium into the bowel lumen. A stool specimen comprised of primarily fluid and flecks of mucous (known as rice water stools) is a distinctive feature when cholera toxin activity is present.
In the absence of mucosal invasion by the bacteria, blood or neutrophils are not found in the stool specimen.
Targeting the conserved regions of the 16s rRNA is commonly used to detect all, but which of the following organisms?
*Streptococcus
pneumoniae
*Chlamydia trachomatis
- Mycobacterium tuberculosis
- Mycoplasma hominis
Streptococcus pneumoniae is the correct answer.
Molecular methods for detecting Streptococcus pneumoniae target multiple genes, including penicillin-binding proteins & lysins. However, 16s rRNA is not typically used.
While the remaining three organisms may be detected through other gene targets, 16s rRNA is commonly used.
A sample has reactions occurring at immediate spin & AHG in a panel that showed varying reaction strengths. There is no obvious pattern that matches a particular panel cell or single antigen profile & the auto-control was negative. Which of the following is the most likely cause?
- An IgM and an IgG antibody
*An IgG antibody only
*An IgM antibody
*An autoantibody
The cause would be the presence of both an IgM & an IgG antibody. Laboratorians should think of multiple antibodies when reactions are occurring at two different phases (IS and AHG), varying strengths in reactions, and no definite patterns. Patterns can sometimes be recognized if you look at each phase individually. For example reactions at IS may match an M antibody, & reactions at AHG may match a D antibody. Varying strengths in reaction could also indicate dosage occurring.
IgM antibodies most often react at IS, room temp, or colder.
IgG antibodies are most often detected at the AHG phase.
Since the autocontrol is negative, the positive reactions are caused by an alloantibody and not autoantibody.
Which of the following are markers currently used to differentiate heart failure from lung disease?
*TnI & TnT
*BNP & NT- proBNP
*Myoglobin & LD
*hs-CRP & homocysteine
BNP & NT-proBNP are currently used to differentiate Heart failure from lung disease.
TnI & TnT are currently used to diagnose acute coronary syndrome & acute myocardial infarction.
Myoglobin & LD are no longer used or are less commonly used as biomarkers for cardiac disease.
hs-CRP & homocysteine are used for cardiovascular risk stratification.
The type of hypersensitivity reaction associated with macrophage activation, cytokine-mediated inflammation is?
- Type 1 Anaphylactic ( Immediate hypersensitivity)
*Type 2 Cytotoxic (Antibody mediated & antibody dependent, complement mediated hypersensitivity)
*Type 3 immune complex mediated hypersensitivity
*Type 4 cell mediated hypersensitivity (T-cell dependent).
Type 4 cell-mediated hypersensitivity is associated with macrophage activation. type 4 is characterized by direct target cell lysis & cytokine-mediated inflammation. There are 3 defining characteristics of type 4 hypersensitivity reactions: (1) Type 4 delayed-type hypersensitivity involving antigen-sensitized T cells or particles that remain phagocytized in a macrophage & are encountered by previously activated T cells for a second or subsequent time. Delayed hypersensitivity is a major defense mechanism again various intracellular pathogens, including mycobacteria, fungi, & certain parasites. (2) Rejection of foreign tissue grafts, elimination of tumor cells bearing neoantigens. (3) Formation of chronic granulomas.
What is the best method for lysing tough bacterial cell walls when the integrity of the chromosomal DNA is important?
*Enzyme digestion
*Bead beating
*Boiling
*Grinding
The correct answer is Enzyme digestion.
Enzymes can be formulated to be gentle enough to lyse cell walls without damaging chromosomal DNA.
Mechanical lysis, such as bead beating and grinding will effectively lyse cell walls but may also damage the DNA.
Boiling will also denature chromosomal DNA to a point where it may not be able to be renatured.
The laboratory test most commonly used to establish a definitive diagnosis of primary syphilis is:
*Rapid plasma reagin (RPR)
*recovery of spirochetes via culture.
*Direct fluorescent antibody test
*Fluorescent treponemal antibody (FTA) with absorption test.
Direct fluorescent antibody test is the definitive method for diagnosis early syphilis. The antibodies produced in response to infection with Treponema pallidum are detectable during primary syphilis. Levels will continue to increase as the disease progresses to secondary syphilis.
The RPR is a screening test. The test detects the presence of cardiolipin and other indicators that correlate to disease activity; however it isn’t highly specific and doesn’t correlate with disease activity.
Spirochetes cannot be recovered outside of the body and thus cannot be cultured.
FTA with absorption is done to diagnose late latent or tertiary syphilis.
What determines the fragment size generated in Sanger sequencing?
*Random incorporation of a ddNTP
*Incorporation of a ddNTP in a specific position
*Random incorporation of a dNTP
*Incorporation of a dNTP in a specific position
The correct answer is random incorporation of a ddNTP.
When chains are synthesized in Sanger sequencing, both dNTPs & ddNTPs are added to the master mix, which one gets added into the sequence is completely random. When a dNTP is added to the chain, it gets extended, but when a ddNTP is added, synthesis stops since ddNTPs lack the oxygen needed to bind the next nucleotide. The random incorporation of these ddNTPs leads to fragments of different lengths.
Which of the following organisms causes Q fever?
*Coxiella burnetii
*Anaplasma spp.
*Orientia tsutsugamushi
*Rickettsia rickettsii
Q fever, an acute systemic infection affecting the lungs, is caused by Coxiella burnetii.
Anaplasma spp. causes granulocytic anaplasmosis.
Orientia tsutsugamushi causes scrub typhus.
Rickettsia rickettsii causes Rocky Mountain spotted fever.
Which of the following laboratories DO NOT belong in the Clinical Pathology Laboratory?
- Histology & Cytology
*Hematology & Coagulation
*Urinalysis & Flow Cytometry
*Immunology & Immunohematology
Histology & Cytology are part of the Anatomical & Surgical Pathology laboratories. Histology is the microscopic study of tissues. In this department, tissues are microscopically examined by pathologist to determine if they are normal or diseased. Cytology is the department where cells in the body tissues & fluids are counted, identified, & studied in order to determine if they are normal, malignant, or premalignant.
Hematology, Coagulation, Urinalysis, Flow Cytometry, Immunology, & Immunohematology, along with Microbiology & Clinical Chemistry, are departments of the Clinical Pathology Laboratories.
Donation of which apheresis blood product more than once every four weeks requires monitoring of total plasma protein & antibody levels?
*Red cell apheresis
*Platelepheresis
*Plasmapheresis
*Leukapheresis
Plasmapheresis is the correct answer. Plasma levels of total protein, IgG, & IgM must be monitored every four months in plasmapheresis donors because levels of these & other proteins present in plasma decrease following plasmapheresis.
Blood components from red cell apheresis, platletpheresis, & leukapheresis do not contain enough volume of plasma to necessitate the monitoring of plasma proteins.
What modification is made to sample DNA during the bisulfite treatment step of bisulfite DNA sequencing?
*Methylated cytosine is deaminated & converted to uracil.
*Unmethylated cytosine is deaminated & converted to uracil.
*Methylated guanine is deaminated & converted to adenine.
*Unmethylated guanine is deaminated & converted to adenine.
The correct answer is Unmethylated cytosine is deaminated & converted to uracil. Bisulfite converts unmethylated cytosine to uracil by removing an amino group.
Methylated cytosine (5-methylcytosine) is unchanged by bisulfite because the methyl group prevents amine from being removed.
Guanine is not epigenetically modified by methylation, so there is no methylated guanine in patient samples.
Unmethylated guanine is not altered by bisulfite
dTTP is replaced by dUTP-UNG system for what purpose?
*Contamination control
*If the starting template is RNA
*Required for RT-PCRs
*Required for nested PCRs
The correct answer is Contamination control. The dUTP-UNG system replaces dTTP with dUTP so that uracil-N-glycosylase (UNG) can be added before the next PCR to degrade any remnant amplicon that could potentially contaminate the next PCR. This is used as a contamination technique.
When RNA is used as the starting template, as is true in RT-PCRs, the DUTP-UNG systemcan be used, but isn’t necessary for the reaction to work, & the standard four dNTPs (A,G,C,T) can still be used. Nested PCRs cannot use the DUTP-UNG system, as the bases of a nested PCR is two back-to-back PCRs, where the amplicon from the first is used as the template for the second- using the DUTP-UNG system would degrade the first PCRs amplicon& leave no template for the second.
Satellitism observed in cultures is most commonly associated with which of the following bacteria?
*Neisseria meningitidis
*Haemophilus influenzae
*Pasteurella canis
*Bordetella pertussis
The correct answer is Haemophilus influenzae
(which requires X factor & V factor) will grow in the hemolytic zone of Staphylococcus aureus on blood agar plates. Sheep blood agar plates (SAP) provide Hamophilus with X factor (hemin) & the hemolysis of RBCs by S. aureus releases V factor (NAD). The X &V factors (hemin & NAD, respectively) diffuse into the surrounding medium & promote the growth of Haemophilus in the area surrounding Staphylococcus colonies in a process called satellitism. For Haemophilus spp., the satellite test substitutes for the V factor test.
Neisseria meningitidis & Pasteurella canis do not have any special growth requirements. They are both able to grow independently on SAP & chocolate agar, but do not grow on MacConkey agar.
Bordetella pertussis requires special medium for isolation, but it isn’t able to obtain any of the required nutrients from the normal growth of other organisms in satellitism.
Current CDC (2014) recommendations for initial HIV screening include FDA-approved immunoassay for detection of?
- HIV-1p31 antigen
*HIV-1 & HIV-2 antibody, HIV-1 p24 antigen
*HIV-1 antibody & HIV-1 gp41 antigen
*HIV-1 & HIV-2 antibody
Fifth generation assays for HIV screening detect three markers: Hiv-1 & HIV-2 antibody, HIV-1 p24 antigen. Antigen detection identifies infection before antibody production occurs. Newer generation assays with sensitivity for HIV-1 p24 antigen can reduce the time between HIV infection and detection.
The Western blot has historically been used for the detection of HIV antibodies to antigens such as p24, p31, gp41, & gp 120/160. However, it is less sensitive than screening test & often demonstrates cross-reactivity. Despite this, it is till used for confirmatory HIV testing.